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无需同步化即可使用流式细胞术对细胞周期进程进行时间追踪。

Temporal Tracking of Cell Cycle Progression Using Flow Cytometry without the Need for Synchronization.

作者信息

Welschinger Robert, Bendall Linda J

机构信息

Centre for Cancer Research, Westmead Millennium Institute for Medical Research and University of Sydney.

Centre for Cancer Research, Westmead Millennium Institute for Medical Research and University of Sydney;

出版信息

J Vis Exp. 2015 Aug 16(102):e52840. doi: 10.3791/52840.

Abstract

This protocol describes a method to permit the tracking of cells through the cell cycle without requiring the cells to be synchronized. Achieving cell synchronization can be difficult for many cell systems. Standard practice is to block cell cycle progression at a specific stage and then release the accumulated cells producing a wave of cells progressing through the cycle in unison. However, some cell types find this block toxic resulting in abnormal cell cycling, or even mass death. Bromodeoxyuridine (BrdU) uptake can be used to track the cell cycle stage of individual cells. Cells incorporate this synthetic thymidine analog, while synthesizing new DNA during S phase. By providing BrdU for a brief period it is possible to mark a pool of cells that were in S phase while the BrdU was present. These cells can then be tracked through the remainder of the cell cycle and into the next round of replication, permitting the duration of the cell cycle phases to be determined without the need to induce a potentially toxic cell cycle block. It is also possible to determine and correlate the expression of both internal and external proteins during subsequent stages of the cell cycle. These can be used to further refine the assignment of cell cycle stage or assess effects on other cellular functions such as checkpoint activation or cell death.

摘要

本方案描述了一种无需使细胞同步化就能追踪细胞通过细胞周期的方法。对于许多细胞系统而言,实现细胞同步化可能具有挑战性。标准做法是在特定阶段阻断细胞周期进程,然后释放积累的细胞,从而产生一波同步通过细胞周期的细胞。然而,某些细胞类型会发现这种阻断具有毒性,导致细胞周期异常,甚至大量死亡。溴脱氧尿苷(BrdU)摄取可用于追踪单个细胞的细胞周期阶段。细胞在S期合成新DNA时会掺入这种合成的胸腺嘧啶类似物。通过在短时间内提供BrdU,有可能标记在BrdU存在时处于S期的一群细胞。然后可以追踪这些细胞在细胞周期的其余阶段以及进入下一轮复制的情况,从而无需诱导潜在有毒的细胞周期阻断就能确定细胞周期各阶段的持续时间。还可以确定并关联细胞周期后续阶段内部和外部蛋白质的表达。这些可用于进一步细化细胞周期阶段的划分,或评估对其他细胞功能(如检查点激活或细胞死亡)的影响。

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